abnormal bone mineralization_Ror2<tm1Anec>/Ror2<tm1Anec>

http://metadb.riken.jp/0002896B6129S1Ror2tm1AnecRor2tm1AnecRor2tm1AnecRor2tm1Anec

abnormal bone mineralization_Ror2<tm1Anec>/Ror2<tm1Anec>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• receptor tyrosine kinase-like orphan receptor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347521

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Ror2<tm1Anec>/Ror2<tm1Anec>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Ror2<tm1Anec>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• B6.129S1-Ror2<tm1Anec>

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• abnormal bone mineralization
  http://purl.obolibrary.org/obo/MP_0002896

文献

http://purl.org/net/cito/citesAsAuthority

• Regina. Raz, et.al., The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome., Development (Cambridge, England), 2008, 135
  http://rdf.ncbi.nlm.nih.gov/pubmed/18353862